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Reaction of 1-methyl-2-phenylindole with nitrogen dioxide or with nitrous acid (NaNO2-CH3COOH) in benzene has been studied. 1-Methyl-2-phenylindole is reported to react with malondialdehyde (MDA) and 4-hydroxyalkenals to afford a stable chromophore with intense maximal absorbance at 586nm. Application Reactant for preparation of: Cyano indoles Difluorohydroxy indoles Reactant for: Carboxylation of indoles Allylation of indoles Formylation of indoles Nitrosylation of indoles 1-Methyl-2-phenylindole may be used in the following studies: The estimation of lipid peroxidation in third instar larvae of transgenic Drosophila melanogaster (hsp70-lacZ)Bg. As chromogenic agent for the determination of estimation of malondialdehyde (MDA) production. Colorimetric assay of lipid peroxidation. Synthesis of 1-methyl-2-phenyl-3-(1,3,4-thiadiazol-2-yldiazenyl)-1H-indole. Synthesis of 3-(5-ethyl-1,3,4-thiadiazol-2-yldiazenyl)-1-methyl-2-phenyl-1H-indole.

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Chinese name

1-甲基-2-苯基吲哚

English name

1-Methyl-2-phenylindole

Chinese alias

1-甲基-2-苯基-1H-吲哚 | N-甲基-2-苯基吲哚

English alias

NSC 63793 | NSC 63793 | AS-59068 | J-504920 | Indole, 1-methyl-2-phenyl- | SY038925 | Z104479722 | BP-13058 | CCRIS 3982 | DTXSID5063073 | STK202660 | AMY23168 | AKOS001426229 | 1-methyl-2-phenyl-1H-indol | UNII-IE3UB978IA | AB00775587-01 | EINECS 222-618

CAS number

3558-24-5

molecular formula

C15H13N

molecular weight

207.27 g/mol

Exact mass

≥99%

PSA

4.900 Å²

Logp

4.100

Technical Documents

3558-24-5 | 1-Methyl-2-phenylindole.pdf
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